A Phase 2 Study to Evaluate Safety and Efficacy of Abiraterone in Participants With Prostate Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

June 6, 2012

Primary Completion Date

October 17, 2014

Study Completion Date

October 17, 2014

Conditions
Prostate Cancer
Interventions
DRUG

Abiraterone

Abiraterone will be administered orally as 1000 milligram (mg) per day for 28-daily dosing cycles which will be continued until disease progression or unacceptable toxicity.

DRUG

Prednisolone

Prednisolone will be administered orally as 5 mg tablets twice daily for 28-daily dosing cycle which will be continued until disease progression or unacceptable toxicity.

Trial Locations (19)

Unknown

Asahi

Fukuoka

Gifu

Kanazawa

Kashiwa

Kita-Gun

Kukichūō

Kurashiki

Maebashi

Matsuyama

Mitaka

Niigata

Osaka

Ōsaka-sayama

Sagamihara

Sakura

Sapporo

Yokohama

Yokosuka

All Listed Sponsors
lead

Janssen Research & Development, LLC

INDUSTRY

NCT01756638 - A Phase 2 Study to Evaluate Safety and Efficacy of Abiraterone in Participants With Prostate Cancer | Biotech Hunter | Biotech Hunter